Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Improving Translational Accuracy02:07

Improving Translational Accuracy

11.9K
Base complementarity between the three base pairs of mRNA codon and the tRNA anticodon is not a failsafe mechanism. Inaccuracies can range from a single mismatch to no correct base pairing at all. The free energy difference between the correct and nearly correct base pairs can be as small as 3 kcal/ mol. With complementarity being the only proofreading step, the estimated error frequency would be one wrong amino acid in every 100 amino acids incorporated. However, error frequencies observed in...
11.9K
Genome-wide Association Studies-GWAS01:11

Genome-wide Association Studies-GWAS

14.4K
Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
14.4K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Insights into the Cross-Population Transferability of Polygenic Scores for Substance Use.

Behavior genetics·2026
Same author

Multi-ancestry transcriptome prediction with functionally informed variants in TOPMed MESA improves performance of transcriptome-wide association studies.

American journal of human genetics·2026
Same author

The association of a common HFE gene variant with stroke disability utilizing predictive machine learning and electronic health records.

Scientific reports·2026
Same author

Integrating axis quantitative trait loci looks beyond cell types and offers insights into brain-related traits.

Nature communications·2025
Same author

An Integrated Large-Scale Atlas of Protein Quantitative Trait Loci across Olink and SomaScan platforms.

medRxiv : the preprint server for health sciences·2025
Same author

IRF7 controls spontaneous autoimmune germinal center and plasma cell checkpoints.

The Journal of experimental medicine·2025
Same journal

Linkage disequilibrium and allelic heterogeneity explain variation in coronary artery disease risk at 9p21 across populations and reduced effect in Africans.

American journal of human genetics·2026
Same journal

Genome-wide association study and predictors of neonatal blood cell traits in Hispanic newborns.

American journal of human genetics·2026
Same journal

Comparison of methods for assessing effects of risk factors on disease progression in Mendelian randomization under index event bias.

American journal of human genetics·2026
Same journal

Deciding "what" to screen for and "when": The importance of natural history information.

American journal of human genetics·2026
Same journal

Homologous recombination deficiency-driven genomic instability in ovarian cancer as an indicator of BRCA1 and BRCA2 variant pathogenicity.

American journal of human genetics·2026
Same journal

Individuals who deviate from polygenic expectation are enriched for damaging variants in genes linked to rare disease.

American journal of human genetics·2026
See all related articles

Related Experiment Video

Updated: Sep 17, 2025

Author Spotlight: Impact of Intergenic Interactions on Disease-Identifying Dark Biomarkers
03:37

Author Spotlight: Impact of Intergenic Interactions on Disease-Identifying Dark Biomarkers

Published on: March 1, 2024

915

TransferTWAS: A transfer learning framework for cross-tissue transcriptome-wide association study.

Daoyuan Lai1, Han Wang2, Tian Gu3

  • 1Department of Statistics and Actuarial Science, School of Computing and Data Science, The University of Hong Kong, Hong Kong SAR, China.

American Journal of Human Genetics
|July 1, 2025
PubMed
Summary
This summary is machine-generated.

Transfer learning-assisted TWAS (TransferTWAS) improves gene-expression prediction for complex traits by adaptively transferring data from genetically similar tissues. This novel framework enhances imputation accuracy and statistical power in transcriptome-wide association studies (TWASs).

Keywords:
eQTLsgenetic associationgenome-wide association studiestranscriptome-wide association studytransfer learning

More Related Videos

A Next-generation Tissue Microarray ngTMA Protocol for Biomarker Studies
09:32

A Next-generation Tissue Microarray ngTMA Protocol for Biomarker Studies

Published on: September 23, 2014

24.2K
iCLIP - Transcriptome-wide Mapping of Protein-RNA Interactions with Individual Nucleotide Resolution
10:45

iCLIP - Transcriptome-wide Mapping of Protein-RNA Interactions with Individual Nucleotide Resolution

Published on: April 30, 2011

58.6K

Related Experiment Videos

Last Updated: Sep 17, 2025

Author Spotlight: Impact of Intergenic Interactions on Disease-Identifying Dark Biomarkers
03:37

Author Spotlight: Impact of Intergenic Interactions on Disease-Identifying Dark Biomarkers

Published on: March 1, 2024

915
A Next-generation Tissue Microarray ngTMA Protocol for Biomarker Studies
09:32

A Next-generation Tissue Microarray ngTMA Protocol for Biomarker Studies

Published on: September 23, 2014

24.2K
iCLIP - Transcriptome-wide Mapping of Protein-RNA Interactions with Individual Nucleotide Resolution
10:45

iCLIP - Transcriptome-wide Mapping of Protein-RNA Interactions with Individual Nucleotide Resolution

Published on: April 30, 2011

58.6K

Area of Science:

  • Genetics
  • Bioinformatics
  • Computational Biology

Background:

  • Transcriptome-wide association studies (TWASs) are crucial for understanding the genetic basis of complex traits.
  • Developing robust gene-expression imputation models for tissues with limited sample sizes presents a significant challenge in TWASs.

Purpose of the Study:

  • To introduce TransferTWAS, a novel framework leveraging transfer learning to enhance gene-expression prediction in TWASs.
  • To improve imputation accuracy and statistical power in multi-tissue TWAS analyses, particularly for tissues with sparse data.

Main Methods:

  • TransferTWAS adaptively transfers information from multiple external tissues to a target tissue using a data-driven weighting strategy.
  • The framework assigns higher weights to genetically similar tissues, outperforming methods that ignore or indirectly model tissue similarity.
  • Performance is evaluated through simulations and analyses of real-world datasets (ROS/MAP, GEUVADIS) and a low-density lipoprotein cholesterol GWAS.

Main Results:

  • TransferTWAS demonstrated superior imputation accuracy compared to existing multi-tissue TWAS methods in simulations.
  • Analyses revealed a substantial gain in statistical power while maintaining robust control over type-I errors.
  • The framework successfully identified more genetic associations for complex traits, including low-density lipoprotein cholesterol, than conventional methods.

Conclusions:

  • TransferTWAS offers a powerful and adaptive approach to multi-tissue gene-expression imputation for TWASs.
  • The method effectively utilizes information from genetically similar tissues, overcoming limitations of existing approaches.
  • TransferTWAS enhances the discovery of genetic associations for complex traits, paving the way for more comprehensive genetic studies.